A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979935



Internal ID20546975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37866536..37869756hg38UCSC Ensembl
chr10:38155464..38158684hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg383221
hg193221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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